Semi-submersible microscope objective with protective element and use of the same in multiphoton imaging method

ABSTRACT

A semi-submersible microscope objective includes a microscope objective having a protective barrel with an optical inlet and optical outlet, and a protective element affixed to the microscope objective, sealing the optical exit but not the optical inlet. A transparent portion of the protective element is aligned with the optical exit. The protective element is separable from the microscope objective without damaging the microscope objective. Use of the semi-submersible microscope objective in a multiphoton imaging method is also disclosed.

TECHNICAL FIELD

The present disclosure broadly relates to microscope objectives andtheir use in multiphoton imaging methods.

BACKGROUND

In a microscope, the objective (sometimes referred to in the art as anobjective lens) is the optical element that gathers light from theobject being observed and focuses the light rays to produce a realimage. For example, the objective lens of a microscope is the one at thebottom near the sample. At its simplest, it is a very high-poweredmagnifying glass, with very short focal length. This is brought veryclose to the specimen being examined so that the light from the specimencomes to a focus inside the microscope tube. The microscope objectiveitself is typically substantially cylindrical or tubular and containsone or more lenses, typically made of glass, confined within aprotective barrel. Microscope objectives generally have an optical inletand optical exit, typically centered along opposite ends of itslongitudinal axis. The optical inlet and optical exit are connected byan optical path extending between them through the microscope objective.

Microscope objectives are typically characterized by two parameters:magnification and numerical aperture. The former typically ranges from4×-100×, while the latter ranges from about 0.1 to 1.4, and focallengths of about 30 millimeters to about 200 microns, respectively.Similarly, microscope objectives with numerical apertures in the rangeof about 0.1 to 1.4 typically have respective working distances (i.e.,the distance between the microscope objective and the focal point whereimaging occurs) of from several millimeters to about 210 microns.Similarly, for high magnification applications, an oil-immersionobjective or water-immersion objective generally has to be used. Theobjective is specially designed to use refractive index matching oil orwater to fill the air gap between the front element and the object toallow the numerical aperture to exceed 1, and hence give greaterresolution at high magnification. Numerical apertures as high as 1.5 oreven higher can be achieved with oil immersion. Microscope objectiveswith high numerical aperture (NA) and of high quality are typicallyquite expensive.

Microscope objectives are also used to focus laser light in a processknown as multiphoton stereolithography. In that process, laser light(typically in the infrared) is focused in a polymerizable compositioncommonly termed a “photoresist”, typically supported on a substrate. Thephotoresist contains a multiphoton absorbing compound, and the laser hassufficiently high power that two (or, less typically, more than two)photons are absorbed essentially simultaneously by the multiphotonabsorbing compound resulting in subsequent polymerization of thephotoresist.

In order to improve resolution, one conventional approach has been topartially submerge the objective lens assembly into a liquid photoresistto eliminate the air interface/objective lens interface. However, thelocalized laser power in multiphoton stereolithography can beconsiderable, and the potential exists for a buildup of polymerizedphotoresist material over time on the microscope objective lens thatcould be difficult to remove from the optical surfaces. Were this tohappen, there is a potential that an expensive microscope objectivecould be rendered unusable.

SUMMARY

In one aspect the present disclosure provides a semi-submersiblemicroscope objective comprising:

-   -   a microscope objective having a protective barrel with an        optical inlet and optical outlet;    -   a protective element affixed to the microscope objective,        sealing the optical exit but not the optical inlet, wherein a        transparent portion of the protective element is aligned with        the optical exit, and wherein the protective element is        separable from the microscope objective without damaging to the        microscope objective.

In another aspect, the present disclosure provides a multiphoton imagingmethod comprising:

-   -   immersing a semi-submersible microscope objective in a liquid        photoresist comprising a multiphoton absorber and a        polymerizable compound, wherein the semi-submersible microscope        objective comprises:        -   a microscope objective having a protective barrel with an            optical inlet and optical outlet;        -   a protective element affixed to the microscope objective,            sealing the optical exit but not the optical inlet, wherein            a transparent portion of the protective element is aligned            with the optical exit, and wherein the protective element is            separable from the microscope objective substantially            without damaging the microscope objective;    -   directing laser light through the semi-submersible microscope        objective and into liquid photoresist in an image-wise manner        under conditions such that multiphoton absorption by the        multiphoton absorber occurs, and at least partial polymerization        of the polymerizable compound occurs resulting in an exposed        photoresist; and    -   developing the exposed photoresist.

Advantageously, semi-submersible objective lens assemblies according tothe present disclosure can be partially submerged in liquid photoresistsduring multiphoton imaging processes, and even in the event that thepolymerizable compound were to polymerize and cause residue buildup onthe microscope objective, relatively mild chemical treatment and/orsimple mechanical disengagement can be used to dislodge it from theexposed (and polymerized) photoresist.

As used herein:

-   -   “light” means electromagnetic radiation having a wavelength in a        range of from about 300 to about 1500 nm;    -   “liquid” refers to a compound that is in a liquid state at one        atmosphere of pressure and at least one temperature in the range        of from 20-25° C., inclusive;    -   “multiphoton absorption” means the simultaneous absorption of        two or more photons of light to reach a photoreactive,        electronic excited state that is energetically inaccessible by        the absorption of a single photon of the same energy;    -   “multiphoton absorber” means a specie capable of undergoing        multiphoton absorption of light;    -   “numeric aperture” means the product of the index of refraction        of the object medium multiplied by the sine of the slope angle        of the outermost ray from an axial point on the object;    -   “optical entrance” refers to the end of a microscope objective        where the light beam has parallel light rays;    -   “optical exit” refers to the end of a microscope objective where        the light beam converges;    -   “photochemically effective amount” means an amount sufficient to        enable the photoreactive species to undergo at least partial        reaction under the selected exposure conditions (as evidenced,        e.g., by a change in density, viscosity, color, pH, refractive        index, or other physical or chemical property);    -   “simultaneous” means two events that occur within the period of        10⁻¹⁴ seconds or less; and    -   “solvent” refers to a nonreactive liquid component of a        composition that dissolves at least one solid component, or        dilutes at least one liquid component, of the composition (in        the case of water, adventitious amounts of water are not        included by the term “solvent”); and    -   “solvent developing” means substantially removing (e.g.,        dissolving) soluble material in a solvent while substantially        not removing insoluble material.

Features and advantages of the present disclosure will be furtherunderstood upon consideration of the detailed description as well as theappended claims.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a schematic exploded perspective view of exemplarysemi-submersible microscope objective 100.

FIG. 2A is a schematic perspective view of protective element 130.

FIG. 2B is a schematic top view of protective element 130.

FIG. 2C is a schematic perspective view cross-sectional view ofprotective element 130.

FIG. 3 is a schematic side view of exemplary semi-submersible microscopeobjective 200.

FIG. 4 is a scanning electron microscopy micrograph generated in Example1.

Repeated use of reference characters in the specification and drawingsis intended to represent the same or analogous features or elements ofthe disclosure. It should be understood that numerous othermodifications and embodiments can be devised by those skilled in theart, which fall within the scope and spirit of the principles of thedisclosure. The figures may not be drawn to scale.

DETAILED DESCRIPTION

The semi-submersible microscope objective can be made by modifying aconventional microscope objective. For use in multiphoton imagingprocesses using liquid photoresists, the numerical aperture (NA) ispreferably at least 1.0, more preferably at least 1.2, and morepreferably at least 1.4, although other numerical apertures may be used,if desired. Objective numerical aperture can be dramatically increasedby designing the objective to be used with an immersion medium, such asoil, glycerin, or water.

Microscope objectives (also known as microscope objective lenses) arewell-known in the art and are commercially available from numeroussources including, for example: Carl Zeiss Microscopy, LLC, Thornwood,N.Y. (e.g., microscope objectives marketed as OBJECTIVE ALPHAPLAN-APOCHROMAT 100×/1.46 OIL DIC M27, OBJECTIVE ANTIFLEX ECPLAN-NEOFLUAR 63×/1.25 OIL PH3 M27, OBJECTIVE ALPHA PLAN-APOCHROMAT100×/1.57 OIL-HI DIC CORR M27, ZEISS 40×/1.0 OIL IRIS MICROSCOPEOBJECTIVE (NA=1.0) and OBJECTIVE ALPHA PLAN-APOCHROMAT 100×/1.46 OILIRIS M27); Nikon Instruments Inc., Melville, N.Y. (e.g., microscopeobjectives marketed as PLAN 100×W (NA=1.1), CFI S FLUOR 40× OIL(NA=1.30), and CFI S FLUOR 100× OIL (NA=0.5-1.3)); and Olympus Corp.,Tokyo, Japan (e.g., microscope objectives marketed as M PLAN APOCHROMATMPLAPON100×O (NA=1.4)).

Advantageously, the present disclosure is especially useful forexpensive microscope objective such as, for example, those designed forimmersion in oil or water and/or having a numerical aperture (NA) of atleast 0.3, at least 0.4, at least 0.5, at least 0.6, at least 0.7, atleast 0.8, at least 0.9, at least 1.0, at least 1.1, at least 1.2, atleast 1.3, or even at least 1.4. In some embodiments, the microscopeobjective has a numerical aperture in a range of from 0.65 to 1.25.

Referring now to FIG. 1, in one embodiment, semi-submersible microscopeobjective 100 comprises microscope objective 110 and protective element130. Microscope objective 110 comprises protective barrel 120, opticalinlet 122, and optical outlet 124 from which laser light emerges fromthe microscope objective during multiphoton stereolithography. Opticalinlet 122 and optical outlet 124 are aligned with centrally disposedlongitudinal axis 128. Protective element 130 is affixed to microscopeobjective 110 such that it seals optical outlet 124 but not opticalinlet 122. Protective element 130 includes transparent portion 132,which is aligned with optical outlet 124.

In the embodiment shown, protective element 130 comprises cap 131 havingcentral opening 133 and sleeve portion 135 extending from cap 131.Sleeve portion 135 is adapted to mechanically engage protective barrel120 of microscope objective 110. Transparent portion 132 comprises glasscover slip 139 secured to cap 131 (e.g., by adhesive or mechanically),which forms a seal protecting the optical outlet from contact with theliquid photoresist during use. Glass cover slip 139 covers centralopening 133 and is adhered to cap 131. The cap and sleeve portions areshown in greater detail in FIG. 1 as being parts of a monolithicprotective element; however, they may comprise separate pieces that areassembled to form part, or all, of the protective element. Furtherdetails concerning protective element 130 are shown in FIGS. 2A-2C.

The protective element may be constructed of any suitable material(s)including, for example: plastic (e.g., polycarbonate, polyimide,polyetherimide (PEI), polyether ether ketone (PEEK), polyester,polyamide, polyurethane, polyolefin (e.g., low molecular weightpolyethylene, high density polyethylene (HDPE), ultrahigh molecularweight polyethylene (UHMWPE), or polypropylene), or polyacetal (e.g.,polyoxymethylene); metal; glass; sapphire; quartz; or a combinationthereof.

Transparent portion 132 may comprise or consist of any transparentmaterial including, for example, glass, quartz, sapphire, plastic, or acombination thereof. While depicted as forming a raised cover over thecentral opening, in may also be disposed flush with the cap or even berecessed within it or disposed on its interior.

Protective element 130 mechanically engages microscope objective 110,and is reversibly affixed to microscope objective 110 using tighteningscrew 136 (see FIG. 2C) which clamps sleeve portion 135 onto protectivebarrel 120. Accordingly, protective element 130 is separable frommicroscope objective 110 without damaging microscope objective 110.

Index-matched fluid 137 (e.g., oil) is disposed between optical outlet124 and glass cover slip 139, thereby eliminating reflections at theinside surface of cover slip 139.

The protective element is affixed to the microscope objective in aremovable manner. That is, it can be separated from the microscopeobjective substantially without damaging the microscope objective.Suitable mechanical means for affixing the protective element to themicroscope objective include, for example, clamps (e.g., as shown inFIG. 1), press fit, repositionable adhesive, and interlocking mechanicalfasteners (e.g., hook and loop fasteners or capped stem fasteners).

In another embodiment, shown in FIG. 3, semi-submersible protectiveelement 200 comprises microscope objective 110 having a transparentprotective coating 232 disposed on a portion thereof. The transparentprotective coating covers and seals optical outlet 124 from contact witha liquid photoresist. To facilitate easy removal without damaging themicroscope objective, the transparent protective coating 232 isdissolvable in a water-based solvent, preferably having a pH in a rangeof from 2 to 16, more preferably from 4 to 10, and even more preferablyfrom 5 to 9.

Preferably, the transparent protective coating comprises a water-solublepolymer Exemplary water-soluble polymers include cold-water-soluble andhot-water-soluble polyvinyl alcohols (preferably cold-water-solubleversions), and water-soluble polymers having pendant carboxyl orcarboxylate groups (e.g., especially those derived from copolymers ofmonomers including acrylic acid, methacrylic acid and/or succinicanhydride). In some embodiments the transparent protective coating maybe chemically and/or physically crosslinked. For example, thetransparent protective coating may comprise a metal ion-crosslinkedacrylic polymer of the type used in commercial vinyl tile floor finishes(e.g., zinc cross-linked acrylic polymer based floor finishes). Themetal crosslinks between acrylic acid or methacrylic acid residues inthis type of floor finish are reversible using aqueous strippers.Aqueous strippers often have an alkaline pH and contain a soluble orcoupled amine (e.g., ethanolamine) that complexes with the metal (e.g.,zinc ion). Metal-free floor finishes are also suitable for use as thetransparent protective coating as they can likewise be readily removedusing an aqueous stripper, optionally with mild rubbing. Water-solublematerials that can be used to form the transparent protective coatinginclude polyvinyl alcohol based materials such as, for example, a 6000grams/mole, 80 percent hydrolyzed polyvinyl alcohol, available as Cat.No. 2225 from Polysciences, Inc., Warrington, Pa., and those polyvinylalcohol based materials described in U.S. Pat. No. 3,087,920 (Suzumuraet al.) and U.S. Pat. No. 8,276,756 (Denome et al.); polyurethanes asdescribed in U.S. Pat. Appl. Pub. No. 2004/0210025 (Hinde et al); andcold water-soluble polyvinyl alcohol/alkyl acrylate copolymers asdisclosed in U.S. Pat. Appl. Pub. No. 2012/0164424.

Floor finish compositions that are strippable using an aqueous strippermay also be used. Suitable floor finish compositions include thosecontaining polyvalent metal ion (e.g., zinc-based floor finishes) thatdevelop chemical crosslinks (e.g., covalent and/or ionic crosslinks)upon drying, and zinc-free floor finish compositions. Examples ofsuitable commercial zinc-free floor finishes and sealers include thoseavailable as SCOTCHGARD UHS 25 FLOOR FINISH, SCOTCHGARD LOW MAINTENANCE25 FLOOR FINISH, SCOTCHGARD LOW MAINTENANCE 18 FLOOR FINISH, and 3MCORNERSTONE FLOOR SEALER/FINISH from 3M Company, Saint Paul, Minn.Examples of suitable strippers include that available as 3M FLOORSTRIPPER and 3M TROUBLESHOOTER LIQUID FINISH REMOVER from 3M Company.

The transparent protective coating can be applied to the microscopeobjective by any suitable method, including brush coating, dip coating,spray coating, spin coating, and wipe coating. Preferably, thetransparent protective coating is applied to a sufficient portion of theprotective barrel that the liquid photoresist will not directly contactthe microscope objective when partially submerged in it during use inmultiphoton imaging (e.g., two-photon stereolithography).

Semi-submersible microscope objectives can be substituted forconventional microscope objectives used in multiphotonstereolithographic processes known in the art.

In general, liquid photoresists comprise a multiphoton absorbingcompound (multiphoton absorber) in combination with at least onepolymerizable compound. In multiphoton stereolithographic processes,laser light is directed through the microscope objective (orsemi-submersible microscope objective in the case of the presentdisclosure) and into liquid photoresist in an image-wise manner underconditions such that multiphoton absorption by the multiphoton absorber,and at least partial polymerization of the polymerizable compound occursresulting in an exposed photoresist. Development of the exposedphotoresist, typically with solvent, then reveals a fabricatedstructure.

Details concerning materials and methods suitable for multiphotonstereolithography using liquid photoresists are described in, forexample, U.S. Pat. Appl. Publ. No. 2012/0218535 (Thiel et al.).Typically, liquid photoresists suitable for conventional one-photonstereolithography (an additive manufacturing process which employs a vatof liquid ultraviolet curable photopolymer resin and an ultravioletlaser to build structures by stepwise formation of layers, one on top ofanother) can be adapted for use as liquid photoresists for multiphotonimaging by replacing the initiator/sensitizer component(s) with onessuitable for multiphoton (e.g., two-photon) imaging. Additional detailscan be found in the examples included hereinbelow. General informationconcerning materials and methods for practicing multiphotonstereolithography can be found, for example, in U.S. Pat. No. 7,118,845(DeVoe et al.).

Advantageously, the semi-submersible microscope objectives of thepresent disclosure can be used in such processes in place of theconventional microscope objective, thereby offering a degree of safetywith respect to accidental adhesion to the photoresist during imaging.

SELECT EMBODIMENTS OF THE PRESENT DISCLOSURE

In a first embodiment, the present disclosure provides asemi-submersible microscope objective comprising:

-   -   a microscope objective comprising:        -   a protective barrel having an optical inlet and an optical            exit; and at least one optical element disposed within the            protective barrel and along an optical path extending            between the optical inlet and the optical exit; and        -   a protective element affixed to the microscope objective,            sealing the optical exit but not the optical inlet, wherein            a transparent portion of the protective element is aligned            with the optical path, and wherein the protective element is            separable from the microscope objective without damaging the            microscope objective.

In a second embodiment, the present disclosure provides asemi-submersible microscope objective according to the first embodiment,wherein the protective element mechanically engages the microscopeobjective.

In a third embodiment, the present disclosure provides asemi-submersible microscope objective according to the secondembodiment, further comprising index-matched fluid disposed between theoptical exit and the transparent portion of the protective element.

In a fourth embodiment, the present disclosure provides asemi-submersible microscope objective according to the first embodiment,wherein the protective element comprises a transparent protectivecoating.

In a fifth embodiment, the present disclosure provides asemi-submersible microscope objective according to the fourthembodiment, wherein the transparent protective coating is dissolvable ina water-based solvent.

In a sixth embodiment, the present disclosure provides asemi-submersible microscope objective according to the fourthembodiment, wherein the transparent protective coating is chemicallycrosslinked.

In a seventh embodiment, the present disclosure provides asemi-submersible microscope objective according to the fourthembodiment, wherein the transparent protective coating comprises atleast one of polyvinyl alcohol or a polymer having pendant carboxyl orcarboxylate groups.

In an eighth embodiment, the present disclosure provides asemi-submersible microscope objective according to the fourthembodiment, wherein the microscope objective has a numerical aperture ofat least 1.0.

In a ninth embodiment, the present disclosure provides a multiphotonimaging method comprising:

-   -   immersing a semi-submersible microscope objective in a liquid        photoresist comprising a multiphoton absorber and a        polymerizable compound, wherein the semi-submersible microscope        objective comprises:        -   a microscope objective comprising:            -   a protective barrel having an optical inlet and an                optical exit; and at least one optical element disposed                within the protective barrel and along an optical path                extending between the optical inlet and the optical                exit; and        -   a protective element affixed to the microscope objective,            sealing the optical exit but not the optical inlet, wherein            a transparent portion of the protective element is aligned            with the optical path, and wherein the protective element is            separable from the microscope objective without damaging the            microscope objective;    -   directing laser light through the semi-submersible microscope        objective and into liquid photoresist in an image-wise manner        under conditions such that multiphoton absorption by the        multiphoton absorber occurs, and at least partial polymerization        of the polymerizable compound occurs resulting in an exposed        photoresist; and    -   developing the exposed photoresist.

In a tenth embodiment, the present disclosure provides a multiphotonimaging method according to the ninth embodiment, wherein the protectiveelement mechanically engages the microscope objective.

In an eleventh embodiment, the present disclosure provides a multiphotonimaging method according to the tenth embodiment, further comprisingindex-matched fluid disposed between the optical exit and thetransparent portion of the protective element.

In a twelfth embodiment, the present disclosure provides a multiphotonimaging method according to the ninth embodiment, wherein the protectiveelement comprises a transparent protective coating.

In a thirteenth embodiment, the present disclosure provides amultiphoton imaging method according to the twelfth embodiment, whereinthe transparent protective coating is dissolvable in a water-basedsolvent.

In a fourteenth embodiment, the present disclosure provides amultiphoton imaging method according to the twelfth embodiment, whereinthe transparent protective coating is chemically crosslinked.

In a fifteenth embodiment, the present disclosure provides a multiphotonimaging method according to the twelfth embodiment, wherein thetransparent protective coating comprises at least one of polyvinylalcohol or a polymer having pendant carboxyl or carboxylate groups.

In a sixteenth embodiment, the present disclosure provides a multiphotonimaging method according to the twelfth embodiment, wherein themicroscope objective has a numerical aperture of at least 1.0.

Objects and advantages of this disclosure are further illustrated by thefollowing non-limiting examples, but the particular materials andamounts thereof recited in these examples, as well as other conditionsand details, should not be construed to unduly limit this disclosure.

EXAMPLES

Unless otherwise noted, all parts, percentages, ratios, etc. in theExamples and the rest of the specification are by weight.

Example 1

In this example, a glass microscope cover slip (about 170-190 microns)was glued to a protective element fabricated from Delrinpolyoxymethylene that clamped directly to the protective barrel of aZeiss 40×/1.0 oil iris microscope objective (available from Carl ZeissMicroscopy, LLC, Thornwood, N.Y.) having a tapered end with a centrallydisposed lens corresponding to the optical outlet when used formultiphoton imaging, and generally shown in FIG. 1. The protectiveelement is shown in FIGS. 2A-2C. The protective element was thenpositioned such that the cover slip was in contact with the lens at theoptical outlet, and a drop of Zeiss IMMERSOL 518F immersion oil wasadded between the lens surface and the cover slip to eliminate air.

Several structures were fabricated using the resultant semi-submersiblemicroscope objective using liquid resists of various compositions. FIG.4 shows a scanning electron microscopy micrograph of some simplegeometric structures that were stacked in the z axis, demonstrating theability to use a lens in liquid resist to write structures taller thanthe working distance of the semi-submersible microscope objective(resulting in the visible seam halfway up the fabricated structure).

The base of the structure in FIG. 4 was written, and then the top halveswere exposed. This sample used 3.5 milliwatts laser power from a Mai Taiultrafast laser (800 nanometer wavelength, <100 femtosecond pulselength, 80 megahertz repetition rate, available from Spectra-Physics,Santa Clara, Calif.) at the focus. The photoresist composition (whichwas liquid) was: 65 parts by weight ERL4221 3,4-epoxycyclohexylmethyl3,4-epoxycyclohexylcarboxylate from Polysciences, Inc., Warrington, Pa.;35 parts by weight of SR351 trimethylolpropane triacrylate from SartomerCo., Exton, Pa.; 0.5 part by weight of2,5-bis[4-(diphenylamino)stryl]-1-(2-ethylhexyloxy)-4-methoxybenzene(KL68) photosensitizer (synthesized as described in U.S. Pat. No.7,265,161 (Leatherdale et al.)); and 1.0 percent by weight of PC-2506diaryliodonium hexafluoroantimonate from Polyset Co., Mechanicville,N.Y., and which has the following structure.

After removal of the protective element, and removal of residual indexmatching oil, no damage to the microscope objective was evident.

Example 2

An oil immersion microscope objective (40× magnification, NA=1.0,available from Carl Zeiss Microscopy, LLC) was coated with a thin layerof polyvinyl alcohol (PVA). A few drops of a 10 percent by weightsolution of PVA in water (6,000 grams/mole, 80% hydrolyzed, Cat. No.22225 from Polysciences, Inc., Warrington, Pa.) was applied to theexposed lens and surrounding metal on the immersion end of themicroscope objective. The microscope objective was manipulated to allowexcess solution to run off the final lens surface to provide a suitablythin transparent protective coating. The coated microscope objective wasplaced in an oven at 50° C. for 2 minutes to facilitate drying.

The coated end of the resultant semi-submersible microscope objectivewas immersed in a liquid photoresist that had been coated on a siliconsubstrate. This resist formulation consisted of: 35 parts by weight ofEPON 828 bisphenol A diglycidyl ether from Momentive, Houston, Tex.; 30parts by weight of ERL4221 3,4-epoxycyclohexylmethyl3,4-epoxycyclohexylcarboxylate from Polysciences, Inc.; and 35 parts byweight of SR351 trimethylolpropane triacrylate for Sartomer Co.; 0.5part of KL68 photosensitizer used in Example 1, and 1 percent by weightof PC-2506 diaryliodonium hexafluoroantimonate from Polyset Co.

A MaiTai ultrafast laser (800 nanometer wavelength, <100 femtosecondpulse length, 80 megahertz repetition rate, available fromSpectra-Physics, Santa Clara, Calif.) was scanned at 10 milliwatts powerat the focal point of the objective lens to fabricate structures in thephotoresist.

After laser scanning, the liquid photoresist sample on silicon wasremoved from the system for development. The liquid photoresistremaining on the objective lens was wiped with lens paper wetted withisopropyl alcohol. The lens coating was examined under an opticalmicroscope and further cleaned with ethyl alcohol and lens paper.Finally the PVA transparent protective coating was removed by immersionin deionized water for 2 minutes. No damage to the microscope objectivewas evident.

Example 3

Example 2 was repeated except that SCOTCHGARD RESILIENT FLOOR PROTECTOR(an aqueous coatable protection product having a solids content of 22percent by weight, a pH of 7.4-8.4, and a viscosity of less than 8centipoise) from 3M Company, Maplewood, Minn., was used in place of thepolyvinyl alcohol solution. After laser scanning, the resist on theobjective lens was wiped with lens paper wetted with isopropyl alcohol,and further cleaned with ethyl alcohol on a lens paper. Finally, thetransparent protective coating was removed by immersion in SpeedStripper Concentrate 6H diluted with water for use with approximatevolume dilution ratio of 1:16 (from 3M Company) for 2 minutes, rinsed indeionized water, and followed by a final rinsing in ethyl alcohol. Nodamage to the microscope objective was evident.

Example 4

Example 2 was repeated, except that SCOTCHGARD LOW MAINTENANCE FLOORFINISH (an aqueous product having a solids content of 25 percent byweight, a pH of 8.1-8.9, and viscosity of less than 10 centipoise) from3M Company, Saint Paul, Minn., was used in place of the polyvinylalcohol solution. After laser scanning, the resist on the objective lenswas wiped with lens paper wetted with isopropyl alcohol, and furthercleaned with ethyl alcohol on a lens paper. Finally, the transparentprotective coating protective coating was removed by immersion in SPEEDSTRIPPER CONCENTRATE 6H (from 3M Company) diluted with water for usewith approximate volume dilution ratio of 1:16 for 2 minutes, rinsed indeionized water, and followed by a final rinsing in ethyl alcohol. Nodamage to the microscope objective was evident.

All cited references, patents, or patent applications in the aboveapplication for letters patent are herein incorporated by reference intheir entirety in a consistent manner. In the event of inconsistenciesor contradictions between portions of the incorporated references andthis application, the information in the preceding description shallcontrol. The preceding description, given in order to enable one ofordinary skill in the art to practice the claimed disclosure, is not tobe construed as limiting the scope of the disclosure, which is definedby the claims and all equivalents thereto.

What is claimed is:
 1. A semi-submersible microscope objectivecomprising: a microscope objective having a protective barrel with anoptical inlet and optical outlet; a protective element affixed to themicroscope objective, covering and sealing the optical outlet but notthe optical inlet, wherein a transparent portion of the protectiveelement is aligned with the optical outlet, wherein the protectiveelement comprises a transparent protective coating, wherein thetransparent protective coating is applied to a portion of the protectivebarrel, and wherein the protective element is separable from themicroscope objective without damaging the microscope objective.
 2. Thesemi-submersible microscope objective of claim 1, wherein thetransparent protective coating is dissolvable in a water-based solvent.3. The semi-submersible microscope objective of claim 1, wherein thetransparent protective coating is chemically crosslinked.
 4. Thesemi-submersible microscope objective of claim 1, wherein thetransparent protective coating comprises at least one of polyvinylalcohol or a polymer having pendant carboxyl or carboxylate groups. 5.The semi-submersible microscope objective of claim 1, wherein themicroscope objective has a numerical aperture in a range of 0.65 to1.25.